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An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy

Corneal confocal microscopy (CCM) derived corneal nerve measures are lower in diabetic sensorimotor polyneuropathy (DSPN). There are, however, methodological challenges in relation to adequate and unbiased sampling of images with objective corneal nerve quantification. Here we compare a new sampling...

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Autores principales: Schaldemose, Ellen L., Hammer, Rasmus E., Ferdousi, Maryam, Malik, Rayaz A., Nyengaard, Jens R., Karlsson, Páll
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387541/
https://www.ncbi.nlm.nih.gov/pubmed/32724219
http://dx.doi.org/10.1038/s41598-020-69314-2
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author Schaldemose, Ellen L.
Hammer, Rasmus E.
Ferdousi, Maryam
Malik, Rayaz A.
Nyengaard, Jens R.
Karlsson, Páll
author_facet Schaldemose, Ellen L.
Hammer, Rasmus E.
Ferdousi, Maryam
Malik, Rayaz A.
Nyengaard, Jens R.
Karlsson, Páll
author_sort Schaldemose, Ellen L.
collection PubMed
description Corneal confocal microscopy (CCM) derived corneal nerve measures are lower in diabetic sensorimotor polyneuropathy (DSPN). There are, however, methodological challenges in relation to adequate and unbiased sampling of images with objective corneal nerve quantification. Here we compare a new sampling method and adjusted area calculation with established methods of corneal nerve quantification in patients with and without DSPN and healthy controls. CCM images from 26 control subjects and 62 patients with type 1 diabetes with (n = 17) and without (n = 45) DSPN were analyzed. The images were randomly selected and corneal nerve fiber length (CNFL), corneal nerve fiber branch density (CNBD) and corneal nerve fiber density (CNFD) were determined in both a manual and automated manner. The new method generated 8–40% larger corneal nerve parameters compared to the standard procedure (p < 0.05). CNFL was significantly reduced using the new method for both manual and automated analysis; whilst CNFD and CNBD were significantly reduced using the automated method in both diabetic groups compared with controls. The new, objective method showed a reduction in corneal nerve parameters in diabetic patients with and without DSPN. We recommend using a randomized sampling method and area-dependent analysis to enable objective unbiased corneal nerve quantification.
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spelling pubmed-73875412020-07-29 An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy Schaldemose, Ellen L. Hammer, Rasmus E. Ferdousi, Maryam Malik, Rayaz A. Nyengaard, Jens R. Karlsson, Páll Sci Rep Article Corneal confocal microscopy (CCM) derived corneal nerve measures are lower in diabetic sensorimotor polyneuropathy (DSPN). There are, however, methodological challenges in relation to adequate and unbiased sampling of images with objective corneal nerve quantification. Here we compare a new sampling method and adjusted area calculation with established methods of corneal nerve quantification in patients with and without DSPN and healthy controls. CCM images from 26 control subjects and 62 patients with type 1 diabetes with (n = 17) and without (n = 45) DSPN were analyzed. The images were randomly selected and corneal nerve fiber length (CNFL), corneal nerve fiber branch density (CNBD) and corneal nerve fiber density (CNFD) were determined in both a manual and automated manner. The new method generated 8–40% larger corneal nerve parameters compared to the standard procedure (p < 0.05). CNFL was significantly reduced using the new method for both manual and automated analysis; whilst CNFD and CNBD were significantly reduced using the automated method in both diabetic groups compared with controls. The new, objective method showed a reduction in corneal nerve parameters in diabetic patients with and without DSPN. We recommend using a randomized sampling method and area-dependent analysis to enable objective unbiased corneal nerve quantification. Nature Publishing Group UK 2020-07-28 /pmc/articles/PMC7387541/ /pubmed/32724219 http://dx.doi.org/10.1038/s41598-020-69314-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schaldemose, Ellen L.
Hammer, Rasmus E.
Ferdousi, Maryam
Malik, Rayaz A.
Nyengaard, Jens R.
Karlsson, Páll
An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title_full An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title_fullStr An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title_full_unstemmed An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title_short An unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
title_sort unbiased stereological method for corneal confocal microscopy in patients with diabetic polyneuropathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387541/
https://www.ncbi.nlm.nih.gov/pubmed/32724219
http://dx.doi.org/10.1038/s41598-020-69314-2
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